 |
 |

Long-term Effects on Plasma Lipids of Diet and Drugs to Treat Hypertension
Richard H. Grimm, Jr, MD, PhD;
John M. Flack, MD, MPH;
Gregory A. Grandits, MS;
Patricia J. Elmer, PhD;
James D. Neaton, PhD;
Jeffrey A. Cutler, MD, MPH;
Cora Lewis, MD;
Robert McDonald, MD;
James Schoenberger, MD;
Jeremiah Stamler, MD;
Treatment of Mild Hypertension Study (TOMHS) Research Group
JAMA. 1996;275(20):1549-1556.
Abstract
 |  |
Objective. —To compare long-term plasma lipid changes among 6 antihypertensive treatment interventions for stage I (mild) hypertension.
Design. —Multicenter, randomized, double-blind, parallel-group clinical trial.
Setting. —Four academic clinical research units in the United States.
Participants. —A total of 902 men and women, aged 45 to 69 years, with stage I diastolic hypertension (diastolic blood pressure <100 mm Hg), recruited from 11 914 persons screened in their communities.
Interventions. —Participants were randomized to 1 of 6 treatment groups: (1) placebo, (2) β-blocker(acebutolol), (3) calcium antagonist (amlodipine), (4) diuretic (chlorthalidone), (5) 1-antagonist (doxazosin), and (6) angiotensin-converting enzyme inhibitor (enalapril). All groups received intensive lifestyle counseling to achieve weight loss, dietary sodium and alcohol reduction, and increased physical activity.
Main Outcomes Measures. —Changes in plasma total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol, and triglycerides from baseline to annual visits through 4 years.
Results. —Mean changes in all plasma lipids were favorable in all groups. The degree of weight loss with fat-modified diet and exercise was significantly related to favorable lipid changes. Significant differences (P<.01) among groups for average changes during follow-up in each lipid were observed. Decreases in plasma total cholesterol and LDL cholesterol were greater with doxazosin and acebutolol (for plasma total cholesterol, 0.36 and 0.30 mmol/L [13.8 and 11.7 mg/dL], respectively), less with chlorthalidone and placebo (0.12 and 0.13 mmol/L [4.5 and 5.1 mg/dL], respectively). Decreases in triglycerides were greater with doxazosin and enalapril, least with acebutolol. Increases in HDL cholesterol were greater with enalapril and doxazosin, least with acebutolol. Significant relative increases in plasma total cholesterol with chlorthalidone compared with placebo at 12 months were no longer present at 24 months and beyond, when mean plasma total cholesterol for the chlorthalidone group fell below baseline. Analyses of participants continuing to receive chlorthalidone throughout the 4 years of follow-up indicated this was not due solely to an increasing percentage of participants changing or discontinuing use of medication during follow-up.
Conclusions. —Weight loss with a fat-modified diet plus increased exercise produces favorable long-term effects on blood pressure and all plasma lipid fractions of adults with stage I hypertension; blood pressure reduction is enhanced to a similar degree by addition of a drug from any one of 5 classes of antihypertensive medication. These drugs differ quantitatively in influencing the degree of long-term favorable effects on blood lipids obtained with nutritional-hygienic treatment.
(JAMA. 1996;275:1549-1556)
Author Affiliations
 |  |
From the Divisions of Cardiology (Dr Grimm) and General Medicine (Dr Flack), Department of Internal Medicine, University of Minnesota Medical School, Minneapolis; Hypertension Center, Bowman-Gray School of Medicine at Wake Forest University, Winston-Salem, NC (Dr Flack); Divisions of Biostatistics (Mr Grandits and Dr Neaton) and Epidemiology (Dr Elmer), School of Public Health, University of Minnesota, Minneapolis; Division of Epidemiology and Clinical Applications, National Heart, Lung, and Blood Institute, Bethesda, Md (Dr Cutler); Department of Medicine, School of Medicine, University of Alabama at Birmingham (Dr Lewis); Department of Medicine, University of Pittsburgh (Pa) (Dr McDonald); Department of Preventive Medicine, Rush-Presbyterian-St Luke's Medical Center, Chicago, Ill (Dr Schoenberger); and Department of Preventive Medicine, Northwestern University Medical School, Chicago, Ill (Dr Stamler). Dr Grimm is now with the Shapiro Center for Evidence-Based Medicine, Minneapolis Medical Research Foundation; Section of Clinical Epidemiology, Department of Medicine, Hennepin County Medical Center, Minneapolis; and Cardiovascular Division, Department of Internal Medicine, University of Minnesota Medical School, Minneapolis.
Footnotes
A complete list of the members of the Treatment of Mild Hypertension Study (TOMHS) Research Group can be found in JAMA. 1993;270:713-724.
Reprint requests: Richard H. Grimm, Jr, MD, PhD, Shapiro Center for Evidence-Based Medicine, 914 S Eighth St, D-5, Minneapolis, MN 55404.
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
 |
Effect of Doxazosin Gastrointestinal Therapeutic System as Third-Line Antihypertensive Therapy on Blood Pressure and Lipids in the Anglo-Scandinavian Cardiac Outcomes Trial
Chapman et al.
Circulation 2008;118:42-48.
ABSTRACT
| FULL TEXT
Old Drug, New Tricks: The Unexpected Effect of Doxazosin on High-Density Lipoprotein
Remaley
Circ. Res. 2007;101:116-118.
FULL TEXT
ATP-Binding Cassette Transporter A1 Gene Transcription Is Downregulated by Activator Protein 2{alpha}: Doxazosin Inhibits Activator Protein 2{alpha} and Increases High-Density Lipoprotein Biogenesis Independent of {alpha}1-Adrenoceptor Blockade
Iwamoto et al.
Circ. Res. 2007;101:156-165.
ABSTRACT
| FULL TEXT
Plasma triglycerides and type III hyperlipidemia are independently associated with premature familial coronary artery disease
Hopkins et al.
J Am Coll Cardiol 2005;45:1003-1012.
ABSTRACT
| FULL TEXT
Effect of Antihypertensive Treatment on PlasmaFibrinogen and Serum HDL Levelsin Patients with Essential Hypertension
Papadakis et al.
CLIN APPL THROMB HEMOST 2005;11:139-146.
ABSTRACT
Value of low dose combination treatment with blood pressure lowering drugs: analysis of 354 randomised trials
Law et al.
BMJ 2003;326:1427.
ABSTRACT
| FULL TEXT
Quinazoline-derived {alpha}1-Adrenoceptor Antagonists Induce Prostate Cancer Cell Apoptosis Via an {alpha}1-Adrenoceptor-independent Action
Benning and Kyprianou
Cancer Res. 2002;62:597-602.
ABSTRACT
| FULL TEXT
Diabetes, Hypertension, and Cardiovascular Disease : An Update
Sowers et al.
Hypertension 2001;37:1053-1059.
ABSTRACT
| FULL TEXT
Angiotensin II Receptor Blockers: Equal or Preferred Substitutes for ACE Inhibitors?
Grossman et al.
Arch Intern Med 2000;160:1905-1911.
FULL TEXT
Exercise and Weight Loss Reduce Blood Pressure in Men and Women With Mild Hypertension: Effects on Cardiovascular, Metabolic, and Hemodynamic Functioning
Blumenthal et al.
Arch Intern Med 2000;160:1947-1958.
ABSTRACT
| FULL TEXT
1999 Canadian recommendations for the management of hypertension
Feldman et al.
CMAJ 1999;161:S1-17.
ABSTRACT
| FULL TEXT
Diuretics and {beta}-Blockers Do Not Have Adverse Effects at 1 Year on Plasma Lipid and Lipoprotein Profiles in Men With Hypertension
Lakshman et al.
Arch Intern Med 1999;159:551-558.
ABSTRACT
| FULL TEXT
{beta}-Blocker-Induced Complications and the Patient With Glaucoma: Newer Treatments to Help Reduce Systemic Adverse Events
Stewart and Garrison
Arch Intern Med 1998;158:221-226.
FULL TEXT
The Sixth Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure
Arch Intern Med 1997;157:2413-2446.
ABSTRACT
Health Outcomes Associated With Antihypertensive Therapies Used as First-Line Agents: A Systematic Review and Meta-analysis
Psaty et al.
JAMA 1997;277:739-745.
ABSTRACT
Efficacy and Safety of Nifedipine Coat-Core versus Amlodipine in Patients With Mild to Moderate Essential Hypertension: Comparison of 24-Hour Mean Ambulatory Diastolic Blood Pressure
Byyny et al.
J CARDIOVASC PHARMACOL THER 1997;2:77-83.
ABSTRACT
SPECIAL JAMA ON HYPERTENSION OFFERS NEW DATA, RECOMMENDATIONS
JWatch General 1996;1996:1-1.
FULL TEXT
High Blood Pressure: Some Answers, New Questions, Continuing Challenges
Lenfant
JAMA 1996;275:1604-1606.
ABSTRACT
|